Table 2.
Gene | Transcript | Exon | Nucleotide change | Alteration | Mutant allele frequency |
---|---|---|---|---|---|
CCND1 | NM_053056 | 1 | c.94C>G | p.L32V | 43.08% |
FLI1 | NM_002017 | 2 | c.196G>A | p.V66I | 44.52% |
ERBB2 | NM_004448 | 20 | c.2313_2324dup | p.772_775dup | 20.66% |
MED12 | NM_005120 | 36 | c.4897G>T | p.E1633* | 3.82% |
* a nonsense mutation in a sequence of DNA that results in a premature stop codon.